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LOW PROFILE GASTROMSTOMY DEVICE

Page Type
Cleared 510(K)
510(k) Number
K923474
510(k) Type
Traditional
Applicant
BIOSEARCH MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
1/5/1993
Days to Decision
175 days
Submission Type
Statement

LOW PROFILE GASTROMSTOMY DEVICE

Page Type
Cleared 510(K)
510(k) Number
K923474
510(k) Type
Traditional
Applicant
BIOSEARCH MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
1/5/1993
Days to Decision
175 days
Submission Type
Statement